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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479127생성일: 2026년 10월 26일

2-Benzoylcyclohexanone → 2-(2-Benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester

https://huagongshe.com/reaction/479127

반응식

참여 물질

역할이름HCID투입량
반응물2-BenzoylcyclohexanoneHCID 275627—
반응물2-Amino-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl esterHCID 69557829—
촉매PalladiumHCID 23938—
용매AnisoleHCID 7519—
생성물2-(2-Benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl esterHCID 6955712115.5%

반응 조건

온도182.5 °C

반응 단계

0.345 g of 2-Amino-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester was dissolved in 6 ml of anisole and treated successively with 0.181 g (1.15 eq.) of 2-benzoyl-cyclohexanone and 60 mg of Pd/C (10%) and heated under Ar to 180-185° C. After 80 Min., additional 60 mg of fresh catalyst was added and heating continued for another 3.5 h. Cooling to RT, pouring onto crashed ice, twofold extraction with AcOEt, washing with water, drying over sodium sulfate, and purification by flash chromatography (SiO2, hexane/AcOEt 7/3) produced 0.075 g of the title compound in the less polar fractions and 0.285 g of intermediate enamine, which was processed once again as just described. Final purification left a combined crop of 0.221 g of 2-(2-benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester as yellow, sticky oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642389B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-5090fdba31e7417fbcbb4338bb908c19
출처 메모uspto-grants-2003_11